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Our data is continuously updated and sourced from EUDAMED, the European database for medical devices and in vitro diagnostics.

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YPSILON® FLOW ½ W COMFORTPAD — 8 UDI-DI variants, MDR

MD Atlas
Camp Scandinavia AB

Data from EUDAMED, last updated May 30, 2026

YPSILON® FLOW ½ W COMFORTPAD

733094538880EC

8 UDI-DI variants

MDR [Regulation (EU) 2017/745 on medical devices]Class I

Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class I
Manufacturer: Camp Scandinavia AB

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Device characteristics

No device characteristics flagged

Identity & classification

Basic UDI-DI: 733094538880EC
Device name: YPSILON® FLOW ½ W COMFORTPAD
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class I
Version date: Apr 22, 2024

Manufacturer & authorised representative

Manufacturer

Name: Camp Scandinavia AB
SRN: SE-MF-000021395
Country: Sweden
Email: info@camp.se
Phone: +4642252700

Variants by status

UDI-DI variants

8 UDI-DI variants

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Applied filters

basicUdiUlid01HW2T0005FT74FSE6J6D4BK18

Format

Summary

29 columns included

Trade name
Basic UDI-DI
UDI-DI code
Risk category
Applicable legislation
Status
Organization name
SRN
Reference / catalog number
Additional product description
Intended medical purpose
Placed on the market (country)
Market info update date
Sterile
Single use
Contains latex
Reprocessed single-use
Direct marking
CMR substance
Endocrine disruptor
Annex XVI applicable
Sterilization
OEM applicable
EMDN codes
Last updated
Basic UDI-DI device name
Basic UDI-DI device model
Basic UDI-DI implantable
Basic UDI-DI reagent

YPSILON® FLOW ½ W COMFORTPAD07330945771141
YPSILON® FLOW ½ W COMFORTPAD07330945771172
YPSILON® FLOW ½ W COMFORTPAD07330945771202
YPSILON® FLOW ½ W COMFORTPAD07330945771189
YPSILON® FLOW ½ W COMFORTPAD07330945771196
YPSILON® FLOW ½ W COMFORTPAD07330945771158
YPSILON® FLOW ½ W COMFORTPAD07330945771134
YPSILON® FLOW ½ W COMFORTPAD07330945771165